List of variants in gene TNIK reported as uncertain significance for autosomal recessive non-syndromic intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_015028.4(TNIK):c.2869A>G (p.Met957Val)	rs200347488	0.00012
NM_015028.4(TNIK):c.1633C>T (p.Arg545Trp)
NM_015028.4(TNIK):c.2724G>T (p.Thr908=)	rs377530882
NM_015028.4(TNIK):c.2729G>A (p.Gly910Glu)	rs35090763
NM_015028.4(TNIK):c.2737A>C (p.Lys913Gln)	rs1340420482

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